Elevate your career in clinical research with Parexel FSP as a Clinical Study Administrator in a hybrid role based in Mississauga, Ontario. This position focuses on coordinating study activities from start to close. As a Clinical Study Administrator, you'll support the Local Study Team by managing essential study documents and ensuring compliance with ICH-GCP guidelines.

Key skills include organizational and administrative expertise, along with proficiency in computer systems.

Your role is crucial in maintaining study timelines and quality objectives. Key Responsibilities:
Coordinate study activities from start-up to closeout
Manage submission of documents to EC/IRB and Regulatory Authorities




Interface with Investigators and CRAs for data collection
Maintain the local eTMF and ISF for compliance
Prepare site-level contract materials as needed Requirements:
High school/Secondary school qualifications
Administrative experience in medical/life sciences
Proven organizational and administration skills
Proficient in English, both written and spoken
Valuable interpersonal skills for international teamwork Bring your administrative skills and attention to detail to Parexel FSP and contribute to impactful clinical studies.

📌 Clinical Study Administrator In Mississauga
🏢 Parexel International
📍 Mississauga